Long-Term Outcomes of Congenital Adrenal Hyperplasia
Nordenström, Anna, Lajic, Svetlana, Falhammar, Henrik
Published in Endocrinology and metabolism (Seoul) (01.08.2022)
Published in Endocrinology and metabolism (Seoul) (01.08.2022)
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Therapy options for adrenal insufficiency and recommendations for the management of adrenal crisis
Nowotny, Hanna, Ahmed, S. Faisal, Bensing, Sophie, Beun, Johan G., Brösamle, Manuela, Chifu, Irina, Claahsen van der Grinten, Hedi, Clemente, Maria, Falhammar, Henrik, Hahner, Stefanie, Husebye, Eystein, Kristensen, Jette, Loli, Paola, Lajic, Svetlana, Reisch, Nicole
Published in Endocrine (01.03.2021)
Published in Endocrine (01.03.2021)
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Rescue of defective G protein-coupled receptor function in vivo by intermolecular cooperation
Rivero-Müller, Adolfo, Chou, Yen-Yin, Ji, Inhae, Lajic, Svetlana, Hanyaloglu, Aylin C, Jonas, Kim, Rahman, Nafis, Ji, Tae H, Huhtaniemi, Ilpo
Published in Proceedings of the National Academy of Sciences - PNAS (02.02.2010)
Published in Proceedings of the National Academy of Sciences - PNAS (02.02.2010)
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Good overall behavioural adjustment in children and adolescents with classic congenital adrenal hyperplasia
Messina, Valeria, Hirvikoski, Tatja, Karlsson, Leif, Vissani, Sophia, Wallensteen, Lena, Ortolano, Rita, Balsamo, Antonio, Nordenström, Anna, Lajic, Svetlana
Published in Endocrine (01.05.2020)
Published in Endocrine (01.05.2020)
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Changes in resting-state functional connectivity in patients with congenital adrenal hyperplasia
Messina, Valeria, van't Westeinde, Annelies, Padilla, Nelly, Lajic, Svetlana
Published in NeuroImage clinical (01.01.2022)
Published in NeuroImage clinical (01.01.2022)
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The Success of a Screening Program Is Largely Dependent on Close Collaboration between the Laboratory and the Clinical Follow-Up of the Patients
Lajic, Svetlana, Karlsson, Leif, Zetterström, Rolf H, Falhammar, Henrik, Nordenström, Anna
Published in International journal of neonatal screening (01.09.2020)
Published in International journal of neonatal screening (01.09.2020)
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Very long‐chain acyl‐CoA dehydrogenase deficiency in a Swedish cohort: Clinical symptoms, newborn screening, enzyme activity, and genetics
Olsson, David, Barbaro, Michela, Haglind, Charlotte, Halldin, Maria, Lajic, Svetlana, Tucci, Sara, Zetterström, Rolf H., Nordenström, Anna
Published in JIMD reports (01.03.2022)
Published in JIMD reports (01.03.2022)
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An update on the long-term outcomes of prenatal dexamethasone treatment in congenital adrenal hyperplasia
van't Westeinde, Annelies, Karlsson, Leif, Messina, Valeria, Wallensteen, Lena, Broesamle, Manuela, Dal Maso, Giorgio, Lazzerini, Alessandro, Kristensen, Jette, Kwast, Diana, Tschaidse, Lea, Auer, Matthias K., Nowotny, Hanna F., Persani, Luca, Reisch, Nicole, Lajic, Svetlana
Published in Endocrine Connections (01.04.2023)
Published in Endocrine Connections (01.04.2023)
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Novel Mutations in CYP21 Detected in Individuals with Hyperandrogenism
Lajić, Svetlana, Clauin, Séverine, Robins, Tiina, Vexiau, Patrick, Blanché, Hélène, Bellanne-Chantelot, Christine, Wedell, Anna
Published in The journal of clinical endocrinology and metabolism (01.06.2002)
Published in The journal of clinical endocrinology and metabolism (01.06.2002)
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Functional and Structural Consequences of Nine CYP21A2 Mutations Ranging from Very Mild to Severe Effects
de Paula Michelatto, Débora, Karlsson, Leif, Lusa, Ana Letícia Gori, Silva, Camila D’Almeida Mgnani, Östberg, Linus Joakim, Persson, Bengt, Guerra-Júnior, Gil, Lemos-Marini, Sofia Helena Valente de, Barbaro, Michela, de Mello, Maricilda Palandi, Lajic, Svetlana
Published in International Journal of Endocrinology (01.01.2016)
Published in International Journal of Endocrinology (01.01.2016)
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Journal Article
Characterization of novel missense mutations in CYP21 causing congenital adrenal hyperplasia
ROBINS, Tiina, BELLANNE-CHANTELOT, Christine, BARBARO, Michela, CABROL, Sylvie, WEDELL, Anna, LAJIC, Svetlana
Published in Journal of molecular medicine (Berlin, Germany) (01.03.2007)
Published in Journal of molecular medicine (Berlin, Germany) (01.03.2007)
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Journal Article
Novel mutations in CYP21 detected in individuals with hyperandrogenism
LAJIC, Svetlana, CLAUIN, Séverine, ROBINS, Tiina, VEXIAU, Patrick, BLANCHE, Hélène, BELIANNE-CHANTELOT, Christine, WEDELL, Anna
Published in The journal of clinical endocrinology and metabolism (01.06.2002)
Published in The journal of clinical endocrinology and metabolism (01.06.2002)
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Journal Article
Congenital adrenal hyperplasia
Auer, Matthias K, Nordenström, Anna, Lajic, Svetlana, Reisch, Nicole
Published in The Lancet (British edition) (21.01.2023)
Published in The Lancet (British edition) (21.01.2023)
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Resting-state functional connectivity in Autoimmune Addison's Disease
van't Westeinde, Annelies, Padilla, Nelly, Lajic, Svetlana
Published in PSYCHONEUROENDOCRINOLOGY (01.07.2023)
Published in PSYCHONEUROENDOCRINOLOGY (01.07.2023)
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Journal Article
Conference Proceeding
CYP21 mutations in simple virilizing congenital adrenal hyperplasia
LAJIC, Svetlana, ROBINS, Tiina, KRONE, Nils, SCHWARZ, Hans P, WEDELL, Anna
Published in Journal of molecular medicine (Berlin, Germany) (01.10.2001)
Published in Journal of molecular medicine (Berlin, Germany) (01.10.2001)
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